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Greig Cephalopolysyndactyly Syndrome: A Family Report
| Content Provider | Semantic Scholar |
|---|---|
| Author | Alp, Hayrullah Alp, Esma Çimen, Derya Oran, Bülent |
| Copyright Year | 2010 |
| Abstract | *Neonatal Intensive Care Unit, Erzurum Nenehatun Obstetrics and Gynecology Hospital, Erzurum, Turkey SUMMARY Introduction: The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. Case Report: The patient had high forehead, frontal bossing, macrocephaly, apparent hypertelorism, down-slanting palpebral fissures and a broad nasal root. The feet showed bilateral polydactyly with cutaneous syndactyly of the fifth digits. Conclusion: GCPS is a rare condition with an autosomal dominant mode of inheritance. The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. Presented here is a case of a 1 week old female with typical clinical manifestations of GCPS. (Journal of Current Pediatrics 2011; 9: 47-9) |
| Starting Page | 74 |
| Ending Page | 79 |
| Page Count | 6 |
| File Format | PDF HTM / HTML |
| Volume Number | 19 |
| Alternate Webpage(s) | http://www.turkiyeklinikleri.com/pdf/?pdf=be147e17464e4bb07b5bae3957307aeb |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
